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HRID 1284930作成日:2026年10月27日

Acetonitrile → 4-Fluoro-4'-(N-propyl-carbamyloxy)-alpha-ethyl-benzhydrol

https://huagongshe.com/reaction/1284930

反応式

関与物質

役割名称HCID仕込み量
反応物AcetonitrileHCID 6342—
反応物Potassium CarbonateHCID 11430—
反応物Propyl isocyanateHCID 61033—
反応物4-Fluoro-4'-hydroxy-alpha-ethyl-benzhydrolHCID 14727320—
溶媒EthanolHCID 702—
生成物4-Fluoro-4'-(N-propyl-carbamyloxy)-alpha-ethyl-benzhydrolHCID 14727327—

反応手順

12.3 g. of 4-fluoro-4'-hydroxy-α-ethyl-benzhydrol, 4.68 g. of n-propyl-isocyanate and 0.7 g. of anhydrous, powdered potassium carbonate in 61 ml. of acetonitrile containing 15 μlit. of a 50% aqueous ethanol solution are refluxed under stirring. When the reaction is complete, the reaction mixture is cooled to room temperature, potassium carbonate is filtered off and acetonitrile is distilled off under reduced pressure. The residue is dissolved in benzene, the benzene solution is shaken with a 5% aqueous sodium hydroxide solution and washed to neutral with water. The organic phase is dried over anhydrous magnesium sulfate, filtered, and benzene is distilled off under reduced pressure. Crystallization of the residue from a mixture of ethyl acetate and n-hexane yields 13.6 g. of the desired compound, melting at 107° to 108° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04564630
出典データセットuspto-grants-1986_01
ORD IDord-4d11fe74511e4c3eb171abfda8490584
出典メモuspto-grants-1986_01